Concepedia

Author

William J. Craigen

Baylor College of Medicine

Also Known As

Bernadette Gochuico, Boucher, Richard C., Brendan H. Lee, Brent L. Fogel, Brian Corner, Cynthia M Cooper, Emilie D. Douine, Emily G. Kelley, Gary D Clark, Gary D. Clark

204

Publications

14.9K

Citations

61

H-Index

172

Concepts

All Affiliations

Baylor College of MedicineBaylor GeneticsTexas Children's HospitalBoston Children's HospitalColumbia University
WJ

About

William J. Craigen is an author at Baylor College of Medicine specializing in medicine, genetics, and pathology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

47

77

7.3K

2

Natural Sciences

14

16

1.9K

3

Health Sciences

3

3

200

4

Engineering

2

2

261

5

Language Studies

1

1

98

William J. Craigen

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122

Publications

13.5K

Citations

56

H-Index

YearCitations

Molecular Findings Among Patients Referred for Clinical Whole-Exome Sequencing

Yaping Yang, Donna M. Muzny, Fan Xia,

JAMA

2014

1.4K

Voltage-dependent anion channels are dispensable for mitochondrial-dependent cell death

Christopher Baines, Robert A. Kaiser, Tatiana Sheiko,

Nature Cell Biology

2007

962

VDAC2 Inhibits BAK Activation and Mitochondrial Apoptosis

Emily H. Cheng, Tatiana Sheiko, Jill K. Fisher,

Science

2003

816

Clinical Characterization of Left Ventricular Noncompaction in Children

Ricardo H. Pignatelli, Colin J. McMahon, William J. Dreyer,

Circulation

2003

649

Clinical Spectrum, Morbidity, and Mortality in 113 Pediatric Patients With Mitochondrial Disease

Fernando Scaglia, Jeffrey A. Towbin, William J. Craigen,

PEDIATRICS

2004

460

Use of Exome Sequencing for Infants in Intensive Care Units

Linyan Meng, Mohan Pammi, Anirudh Saronwala,

JAMA Pediatrics

2017

422

Spectrum of CHD7 Mutations in 110 Individuals with CHARGE Syndrome and Genotype-Phenotype Correlation

Seema R. Lalani, Arsalan M. Safiullah, Susan Fernbach,

The American Journal of Human Genetics

2006

391

Mutations in the <i>DNAH11</i> (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia

Lucia Bartoloni, Jean‐Louis Blouin, Yanzhen Pan,

Proceedings of the National Academy of Sciences

2002

359

Genetic Predictors and Remodeling of Dilated Cardiomyopathy in Muscular Dystrophy

John L. Jefferies, Benjamin W. Eidem, John W. Belmont,

Circulation

2005

281

Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males

Daniela del Gaudio, Ping Fang, Fernando Scaglia,

Genetics in Medicine

2006

269

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